Shiono T - Search Results

1

Autosomal dominant cone-rod dystrophy with negative electroretinogram.

Fujii N, Shiono T, Wada Y, Nakazawa M, Tamai M, Yamada N. Fujii N, et al. Among authors: shiono t. Br J Ophthalmol. 1995 Oct;79(10):916-21. doi: 10.1136/bjo.79.10.916. Br J Ophthalmol. 1995. PMID: 7488580 Free PMC article.

2

Novel 615delC mutation in the CRX gene in a Japanese family with cone-rod dystrophy.

Itabashi T, Wada Y, Sato H, Kawamura M, Shiono T, Tamai M. Itabashi T, et al. Among authors: shiono t. Am J Ophthalmol. 2004 Nov;138(5):876-7. doi: 10.1016/j.ajo.2004.05.067. Am J Ophthalmol. 2004. PMID: 15531334

3

Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin gene.

Shiono T, Hotta Y, Noro M, Sakuma T, Tamai M, Hayakawa M, Hashimoto T, Fujiki K, Kanai A, Nakajima A. Shiono T, et al. Jpn J Ophthalmol. 1992;36(1):69-75. Jpn J Ophthalmol. 1992. PMID: 1635298

4

Analysis of rhodopsin gene in patients with retinitis pigmentosa using allele-specific polymerase chain reaction.

Nakazawa M, Kikawa-Araki E, Shiono T, Tamai M. Nakazawa M, et al. Among authors: shiono t. Jpn J Ophthalmol. 1991;35(4):386-93. Jpn J Ophthalmol. 1991. PMID: 1668242

5

Pattern dystrophy of the retinal pigment epithelium.

Shiono T, Ishikawa A, Hara S, Tamai M. Shiono T, et al. Retina. 1990;10(4):251-4. doi: 10.1097/00006982-199010000-00004. Retina. 1990. PMID: 2089542

6

X linked ocular albinism in Japanese patients.

Shiono T, Tsunoda M, Chida Y, Nakazawa M, Tamai M. Shiono T, et al. Br J Ophthalmol. 1995 Feb;79(2):139-43. doi: 10.1136/bjo.79.2.139. Br J Ophthalmol. 1995. PMID: 7696233 Free PMC article.

7

Ocular findings in patients with autosomal dominant retinitis pigmentosa and transversion mutation in codon 244 (Asn244Lys) of the peripherin/RDS gene.

Nakazawa M, Kikawa E, Kamio K, Chida Y, Shiono T, Tamai M. Nakazawa M, et al. Among authors: shiono t. Arch Ophthalmol. 1994 Dec;112(12):1567-73. doi: 10.1001/archopht.1994.01090240073028. Arch Ophthalmol. 1994. PMID: 7993211

8

Autosomal dominant cone-rod dystrophy associated with mutations in codon 244 (Asn244His) and codon 184 (Tyr184Ser) of the peripherin/RDS gene.

Nakazawa M, Kikawa E, Chida Y, Wada Y, Shiono T, Tamai M. Nakazawa M, et al. Among authors: shiono t. Arch Ophthalmol. 1996 Jan;114(1):72-8. doi: 10.1001/archopht.1996.01100130068011. Arch Ophthalmol. 1996. PMID: 8540854

9

Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP).

Fujiki K, Hotta Y, Hayakawa M, Sakuma H, Shiono T, Noro M, Sakuma T, Tamai M, Hikiji K, Kawaguchi R, et al. Fujiki K, et al. Among authors: shiono t. Jpn J Hum Genet. 1992 Jun;37(2):125-32. doi: 10.1007/BF01899733. Jpn J Hum Genet. 1992. PMID: 1391967

10

Vitreous, retinal and subretinal hemorrhages associated with von Willebrand's syndrome.

Shiono T, Abe S, Watabe T, Noro M, Tamai M, Akutsu Y, Ishikawa M, Suzuki S, Mori K. Shiono T, et al. Graefes Arch Clin Exp Ophthalmol. 1992;230(5):496-7. doi: 10.1007/BF00175940. Graefes Arch Clin Exp Ophthalmol. 1992. PMID: 1521819

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